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. 2018 Feb 23;22(2):135–143. doi: 10.4196/kjpp.2018.22.2.135

Fig. 7. Effects of LPS on the MAPK pathway in LPS-treated HK-2 cells.

Fig. 7

Expression of pP38 tended to increase in LPS-treated mice and phosphorylation of P38, c-Jun N-terminal kinase (pJNK), and extracellular signal-regulated kinase (pERK 1/2) increased in LPS-treated HK-2 cells, and was attenuated by TAPI1 and TAPI2 treatment. Increased phosphorylation of ERK 1/2 was not affected by TAPI1 treatment. Results are presented as mean±SEM of three individual experiments. *p<0.05 vs. control. #p<0.05 vs. LPS.